Antibody data
- Antibody Data
- Antigen structure
- References [2]
- Comments [0]
- Validations
- Western blot [3]
- Immunocytochemistry [1]
- Other assay [1]
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- Product number
- PA5-17215 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- SIRT6 Polyclonal Antibody
- Antibody type
- Polyclonal
- Antigen
- Synthetic peptide
- Description
- It is not recommended to aliquot this antibody. This antibody is not cross-reactive with other sirtuin proteins.
- Reactivity
- Human
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 100 µL
- Concentration
- 16 µg/mL
- Storage
- -20°C
Submitted references Natural polyphenols as sirtuin 6 modulators.
Myeloid deletion of SIRT1 induces inflammatory signaling in response to environmental stress.
Rahnasto-Rilla M, Tyni J, Huovinen M, Jarho E, Kulikowicz T, Ravichandran S, A Bohr V, Ferrucci L, Lahtela-Kakkonen M, Moaddel R
Scientific reports 2018 Mar 7;8(1):4163
Scientific reports 2018 Mar 7;8(1):4163
Myeloid deletion of SIRT1 induces inflammatory signaling in response to environmental stress.
Schug TT, Xu Q, Gao H, Peres-da-Silva A, Draper DW, Fessler MB, Purushotham A, Li X
Molecular and cellular biology 2010 Oct;30(19):4712-21
Molecular and cellular biology 2010 Oct;30(19):4712-21
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Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Knockdown of SIRT6 was achieved by transfecting A549 cells with SIRT6 specific siRNAs (Silencer® select Product # s195228, s28306). Western blot analysis (Fig. a) was performed using modified whole cell extracts (1% SDS) from the SIRT6 knockdown cells (lane 2) and non-target siRNA transfected cells (lane 1). The blot was probed with SIRT6 Polyclonal Antibody (Product # PA5-17215, 1:1000 dilution) and Goat anti-Rabbit IgG (H+L) Superclonal™ Secondary Antibody, HRP conjugate (Product # A27036, 0.25µg/ml, 1:4000 dilution). Densitometric analysis of this western blot is shown in histogram (Fig. b). Decrease in signal upon siRNA mediated knock down confirms that antibody is specific to SIRT6.
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Western blot analysis of SirT6 in Hela and Jurkat cells using SirT6 polyclonal antibody (Product # PA5-17215).
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Western blot analysis was performed on modified whole cell extracts (1% SDS) (30 µg lysate) of A549 (Lane 1), MCF7 (Lane 2), HCT 116 (Lane 3), Jurkat (Lane 4), HeLa (Lane 5), iPSC (Lane 6) and Embryoid Bodies (Lane 7). The blot was probed with Anti-SIRT6 Polyclonal Antibody (Product # PA5-17215, 1:1000 dilution) and detected by chemiluminescence using Goat anti-Rabbit IgG (H+L) Superclonal™ Secondary Antibody, HRP conjugate (Product # A27036, 0.25 µg/ml, 1:4000 dilution). A 45 kDa band corresponding to SIRT6 was observed across the cell lines tested.
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Immunofluorescence analysis of SIRT6 was performed using 70% confluent log phase A549 cells. The cells were fixed with 4% paraformaldehyde for 10 minutes, permeabilized with 0.1% Triton™ X-100 for 15 minutes, and blocked with 1% BSA for 1 hour at room temperature. The cells were labeled with SIRT6 Polyclonal Antibody (Product # PA5-17215) at 1:100 dilution in 0.1% BSA, incubated at 4 degree Celsius overnight and then labeled with Goat anti-Rabbit IgG (H+L) Superclonal™ Secondary Antibody, Alexa Fluor® 488 conjugate (Product # A27034) at a dilution of 1:2000 for 45 minutes at room temperature (Panel a: green). Nuclei (Panel b: blue) were stained with SlowFade® Gold Antifade Mountant with DAPI (Product # S36938). F-actin (Panel c: red) was stained with Rhodamine Phalloidin (Product # R415, 1:300). Panel d represents the merged image showing nuclear localization. Panel e represents control cells with no primary antibody to assess background. The images were captured at 60X magnification.
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- NULL